rs104894263

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;C)	0	common in clinvar
(C;G)	5.8	Multiple Endocrine Neoplasia Type 1

Make rs104894263(G;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

64809695

Gene

MEN1

is a	snp
is	mentioned by
dbSNP	rs104894263
dbSNP (classic)	rs104894263
ClinGen	rs104894263
ebi	rs104894263
HLI	rs104894263
Exac	rs104894263
Gnomad	rs104894263
Varsome	rs104894263
LitVar	rs104894263
Map	rs104894263
PheGenI	rs104894263
Biobank	rs104894263
1000 genomes	rs104894263
hgdp	rs104894263
ensembl	rs104894263
geneview	rs104894263
scholar	rs104894263
google	rs104894263
pharmgkb	rs104894263
gwascentral	rs104894263
openSNP	rs104894263
23andMe	rs104894263
SNPshot	rs104894263
SNPdbe	rs104894263
MSV3d	rs104894263
GWAS Ctlg	rs104894263

Max Magnitude

5.8

OMIM	131100
Desc
Variant	0023
Related	also

ClinVar
Risk	rs104894263(G;G)
Alt	rs104894263(G;G)
Reference	Rs104894263(C;C)
Significance	Pathogenic
Disease	Multiple endocrine neoplasia Hereditary cancer-predisposing syndrome
Variation	info
Gene	MEN1
CLNDBN	Multiple endocrine neoplasia, type 1 Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000011.9:g.64577167G>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000018179.3, RCV000491226.1,